Literature DB >> 8592300

Neurons with different temporal firing patterns in the inferior colliculus of the little brown bat differentially process sinusoidal amplitude-modulated signals.

C J Condon1, K R White, A S Feng.   

Abstract

We examined how well single neurons in the inferior colliculus (IC) of an FM bat (Myotis lucifugus) processed simple tone bursts of different duration and sinusoidal amplitude-modulated (SAM) signals that approximated passively heard natural sounds. Units' responses to SAM tones, measured in terms of average spike count and firing synchrony to the modulation envelope, were plotted as a function of the modulation frequency to construct their modulation transfer functions. These functions were classified according to their shape (e.g., band-, low-, high-, and all-pass). IC neurons having different temporal firing patterns to simple tone bursts (tonic, chopper, onset-late, and onset-immediate) exhibited different selectivities for SAM signals. All tonic and 83% of chopper neurons responded robustly to SAM signals and displayed a variety of spike count-based response functions. These neurons showed a decreased level of time-locking as the modulation frequency was increased, and thereby gave low-pass synchronization-based response functions. In contrast, 64% of onset-immediate, 37% of onset-late and 17% of chopper units failed to respond to SAM signals at any modulation frequency tested (5-800 Hz). Those onset neurons that did respond to SAM showed poor time-locking (i.e., non-significant levels of synchronization). We obtained evidence that the poor SAM response of some onset and chopper neurons was due to a preference for short-duration signals. These data suggest that tonic and most chopper neurons are better-suited for the processing of long-duration SAM signals related to passive hearing, whereas onset neurons are better-suited for the processing of short, pulsatile signals such as those used in echolocation.

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Year:  1996        PMID: 8592300     DOI: 10.1007/bf00188158

Source DB:  PubMed          Journal:  J Comp Physiol A            Impact factor:   1.836


  39 in total

1.  Response timing constraints on the cortical representation of sound time structure.

Authors:  D P Phillips; S E Hall
Journal:  J Acoust Soc Am       Date:  1990-09       Impact factor: 1.840

2.  Influence of envelope rise time on neural responses in the auditory system of anurans.

Authors:  J C Hall; A S Feng
Journal:  Hear Res       Date:  1988-11       Impact factor: 3.208

3.  Periodicity coding in the inferior colliculus of the cat. I. Neuronal mechanisms.

Authors:  G Langner; C E Schreiner
Journal:  J Neurophysiol       Date:  1988-12       Impact factor: 2.714

4.  Unit responses in the rat cochlear nucleus to repetitive, transient sounds.

Authors:  A R Moller
Journal:  Acta Physiol Scand       Date:  1969-04

5.  Classification of inferior collicular neurones of bats in terms of responses to pure tones, FM sounds and noise bursts.

Authors:  N Suga
Journal:  J Physiol       Date:  1969-02       Impact factor: 5.182

6.  Factors shaping the tone level sensitivity of single neurons in posterior field of cat auditory cortex.

Authors:  D P Phillips; M N Semple; L M Kitzes
Journal:  J Neurophysiol       Date:  1995-02       Impact factor: 2.714

7.  Time and Frequency domain processing in the inferior colliculus of echolocating bats.

Authors:  R D Bodenhamer; G D Pollak
Journal:  Hear Res       Date:  1981-11       Impact factor: 3.208

8.  Coding of small sinusoidal frequency and amplitude modulations in the inferior colliculus of 'CF-FM' bat, Rhinolophus ferrumequinum.

Authors:  G Schuller
Journal:  Exp Brain Res       Date:  1979-01-02       Impact factor: 1.972

9.  The monaural nuclei of the lateral lemniscus in an echolocating bat: parallel pathways for analyzing temporal features of sound.

Authors:  E Covey; J H Casseday
Journal:  J Neurosci       Date:  1991-11       Impact factor: 6.167

10.  Passive sound localization of prey by the pallid bat (Antrozous p. pallidus).

Authors:  Z M Fuzessery; P Buttenhoff; B Andrews; J M Kennedy
Journal:  J Comp Physiol A       Date:  1993-01       Impact factor: 1.836

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  8 in total

1.  Temporal Envelope Coding by Inferior Colliculus Neurons with Cochlear Implant Stimulation.

Authors:  Kenneth E Hancock; Yoojin Chung; Martin F McKinney; Bertrand Delgutte
Journal:  J Assoc Res Otolaryngol       Date:  2017-07-17

2.  Temporal masking reveals properties of sound-evoked inhibition in duration-tuned neurons of the inferior colliculus.

Authors:  Paul A Faure; Thane Fremouw; John H Casseday; Ellen Covey
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

3.  Temporal coding of concurrent acoustic signals in auditory midbrain.

Authors:  D A Bodnar; A H Bass
Journal:  J Neurosci       Date:  1997-10-01       Impact factor: 6.167

4.  Cochlear tuning and the peripheral representation of harmonic sounds in mammals.

Authors:  William P Shofner
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2022-07-22       Impact factor: 2.389

5.  Distinct roles for onset and sustained activity in the neuronal code for temporal periodicity and acoustic envelope shape.

Authors:  Yi Zheng; Monty A Escabí
Journal:  J Neurosci       Date:  2008-12-24       Impact factor: 6.167

6.  Flying in silence: Echolocating bats cease vocalizing to avoid sonar jamming.

Authors:  Chen Chiu; Wei Xian; Cynthia F Moss
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-25       Impact factor: 11.205

7.  Responses to amplitude modulated infrared stimuli in the guinea pig inferior colliculus.

Authors:  Claus-Peter Richter; Hunter Young
Journal:  Proc SPIE Int Soc Opt Eng       Date:  2013-03-08

8.  Cascaded Tuning to Amplitude Modulation for Natural Sound Recognition.

Authors:  Takuya Koumura; Hiroki Terashima; Shigeto Furukawa
Journal:  J Neurosci       Date:  2019-05-15       Impact factor: 6.167

  8 in total

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